| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:416792-416885 | Rare:25 | ||||
| chr11:417021-417213 | Common:1; Rare:40 | ||||
| chr11:417256-417609 | Rare:78 | ||||
| chr11:441616-441675 | Rare:12 | ||||
| chr11:441920-442175 | Common:1; Rare:67 | ||||
| chr11:448046-448507 | Common:3; Rare:131 | ||||
| chr11:450076-450460 | Common:1; Rare:108 | ||||
| chr11:450736-450916 | Common:3; Rare:40 | ||||
| chr11:505659-505930 | Common:4; Rare:52 | ||||
| chr11:506129-506586 | Common:4; Rare:105 | ||||
| chr11:506660-507066 | Common:4; Rare:126 | ||||
| chr11:507093-507619 | Common:4; Rare:163 | ||||
| chr11:535345-535395 | Common:1; Rare:13 | ||||
| chr11:535407-535819 | Common:8; Rare:163; Clinvar (benign):2 | ||||
| chr11:536766-536830 | Common:1; Rare:20 |